ALS deficiency caused by an exon 2 deletion and a novel missense variant in the gene encoding ALS

dc.contributor.authorDominguez Menéndez, Gonzalo
dc.contributor.authorPoggi, Helena
dc.contributor.authorArancibia, Mónica
dc.contributor.authorBenavides, Felipe
dc.contributor.authorMartínez Aguayo, Alejandro Gregorio
dc.date.accessioned2020-11-25T17:33:43Z
dc.date.available2020-11-25T17:33:43Z
dc.date.issued2019
dc.format.extent4 páginas
dc.fuente.origenConveris
dc.identifier.doi10.1016/j.ghir.2019.07.002
dc.identifier.issn1096-6374
dc.identifier.issn1532-2238
dc.identifier.urihttps://doi.org/10.1016/j.ghir.2019.07.002
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/48928
dc.language.isoen
dc.pagina.final8
dc.pagina.inicio5
dc.revistaGrowth Hormone and IGF Researches_ES
dc.rightsacceso restringido
dc.titleALS deficiency caused by an exon 2 deletion and a novel missense variant in the gene encoding ALSes_ES
dc.typeartículo
sipa.codpersvinculados115999
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